7-BIA   Click here for help

GtoPdb Ligand ID: 10109

Synonyms: compound 14 [PMID: 30348770]
Compound class: Synthetic organic
Comment: 7-BIA is a 7-butoxy analogue of illudalic acid (PubChem CID 3653077) that has been reported as an inhibitor of receptor type protein tyrosine phosphatase D (PTPRD) [2], which is a novel therapeutic target for the treatment of addiction.
Click here for help

Ligand Activity Visualisation Charts

These are box plot that provide a unique visualisation, summarising all the activity data for a ligand taken from ChEMBL and GtoPdb across multiple targets and species. Click on a plot to see the median, interquartile range, low and high data points. A value of zero indicates that no data are available. A separate chart is created for each target, and where possible the algorithm tries to merge ChEMBL and GtoPdb targets by matching them on name and UniProt accession, for each available species. However, please note that inconsistency in naming of targets may lead to data for the same target being reported across multiple charts.

✖

View interactive charts of activity data across species
2D Structure
Click here for help

2D Structure

An image of the ligand's 2D structure. For small molecules with SMILES these are drawn using the NCI/CADD Chemical Identifier Resolver. Click on the image to access the chemical structure search tool with the ligand pre-loaded in the structure editor. For other types of ligands, e.g. longer nucleotides and peptides, a manually drawn representation of the molecule may be provided.

✖
Click here for structure editor
Physico-chemical Properties
Click here for help

Physico-chemical Properties

Calculated molecular properties are available for small molecules and natural products (not peptides). Properties were generated using the CDK toolkit. All properties were selected to enable the prediction of the Lipinski Rule-of-Five profile or ‘druglikeness’ for each ligand. For more info on each category see the help pages.

✖
Hydrogen bond acceptors 4
Hydrogen bond donors 1
Rotatable bonds 6
Topological polar surface area 82.06
Molecular weight 294.11
XLogP 1.88
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
Click here for help

SMILES / InChI / InChIKey

SMILES (Simplified Molecular Input Line Entry Specification) A specification for unambiguously describing the structure of chemical molecules using short ASCII strings. Canonical SMILES specify a unique representation of the 2D structure without chiral or isotopic specifications. Isomeric SMILES include chiral specification and isotopes.

Standard InChI (IUPAC International Chemical Identifier) and InChIKey InChI is a non-proprietary, standard, textual identifier for chemical substances designed to facilitate linking of information and database searching. An InChIKey is a simplified version of a full InChI, designed for easier web searching.

✖
Canonical SMILES CCCCOc1cc2C(=O)OC(Cc2c(c1OC)C=O)O
Isomeric SMILES CCCCOc1cc2C(=O)OC(Cc2c(c1OC)C=O)O
InChI InChI=1S/C15H18O6/c1-3-4-5-20-12-6-10-9(7-13(17)21-15(10)18)11(8-16)14(12)19-2/h6,8,13,17H,3-5,7H2,1-2H3
InChI Key DAVCIYWSVYDJKW-UHFFFAOYSA-N
Bioactivity Comments
7-BIA administration in mouse models of cocaine addiction/reward produces results which support inhibition of PTPRD as a tractable mechanistic approach for the development of antiaddiction therapeutics [2].
Selectivity at catalytic receptors
Key to terms and symbols Click column headers to sort
Target Sp. Type Action Value Parameter Concentration range (M) Reference
RTP Type D Primary target of this compound Hs Inhibitor Inhibition 5.5 – 6.0 pIC50 - 2
⤷ pIC50 5.5 – 6.0 (IC50 3x10-6 – 1x10-6 M) [2]
Description: Inhibition of p-nitrophenyl phosphate dephosphorylation by recombinant PTPRD phosphatase domain fusion protein following 16-18 minute preincubation.
RTP Type S Hs Inhibitor Inhibition 4.4 pIC50 - 1
⤷ pIC50 4.4 (IC50 4x10-5 M) [1]
Description: Inhibition of p-nitrophenyl phosphate dephosphorylation by recombinant PTPRS phosphatase domain fusion protein following 16-18 minute preincubation.